The relation of contrast-enhanced transverse relaxation rates R 2 * and R 2 provides in vivo mapping of the mean caliber of cerebral vessels. This technique is referred to as vessel size imaging (VSI) The microvasculature, which includes the smallest and intermediate vessels, cannot be imaged directly with current MRI techniques. MRI examinations yield averaged microvasculature-related characteristics of perfusion or pharmacokinetics. Recently, attempts have been made to measure the mean vessel caliber in vivo (1, 2) in animal models. The feasibility of such measurements is granted by the difference in the contributions of small vessels to the transverse relaxation rates of the free induction decay, R* 2 , and that of the spin echo (SE), R 2 , (3-7) (Fig. 1). The method is based on measuring the changes in both rates, ⌬R* 2 and ⌬R 2 , after administration of a paramagnetic contrast agent. The average vessel size in a tissue can be estimated from ⌬R* 2 and ⌬R 2 according to theoretical predictions provided either by Monte Carlo simulations (2, 3) or by analytical modeling (4,8,9)..A quantitative assessment of the microvasculature might have diagnostic impact on the differential diagnosis of intracranial tumors. In a recent study (5) a correlation was found between glioma grade and regional cerebral blood volume (rCBV) measured with a gradient echo (GE) technique, while SE data showed no significant correlation. This result was qualitatively explained by the higher sensitivity of R* 2 to large vessels, which are inherent to malignant tumor tissues. Similarly, it was reported (6, 7) that the difference in regional blood volume assessed with GE and SE techniques increases for high-grade brain tumors.In the present study, quantitative imaging of the mean vessel caliber was performed in brain tumor patients undergoing routine MRI examinations. Previous experiments were performed in animals (2) using an intravascular contrast agent (USPIO) and monitoring its blood concentration invasively. The present method has been developed to meet the conditions of human studies in a clinical environment, in particular, the transient character of the contrast enhancement during the first bolus passage. The analysis presented and computer simulations help to understand the restrictions of the method and its shortcomings, which are caused by the complex relationship between the microvascular morphology and the measured NMR signal. Four illustrative cases of brain tumors are discussed in the context of the model developed.